1204-54-2 Usage
Structure
A unique structure that includes a furan ring and a dioxane ring.
Physical state
A colorless liquid at room temperature.
Usage
Serves as a solvent and intermediate in the synthesis of pharmaceuticals and organic compounds.
Boiling point
High boiling point, which contributes to its stability and application in various processes.
Solubility
Good solubility in a variety of organic solvents, making it compatible with many chemical reactions and processes.
Flavoring agent
Utilized as a flavoring agent in food and beverages, enhancing taste and aroma.
Chemical properties
The versatile chemical properties of 2-(furan-2-yl)-4,4,6-trimethyl-1,3-dioxane make it valuable in various industrial applications, including the production of pharmaceuticals, organic compounds, and flavorings.
Check Digit Verification of cas no
The CAS Registry Mumber 1204-54-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,0 and 4 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1204-54:
(6*1)+(5*2)+(4*0)+(3*4)+(2*5)+(1*4)=42
42 % 10 = 2
So 1204-54-2 is a valid CAS Registry Number.
1204-54-2Relevant academic research and scientific papers
Melnitskaya,Kuramshin,Khlebnikova,Melnitskii,Kantor
, p. 908 - 914 (1997)
Quantum chemical calculations and the PMR method are used to show that the preferable conformation of cyclic furfural acetals is a chair with an axial orientation of the furyl substituent. In 2-(furyl-2′)-5-ethyl-5-oxymethyl-1,3-dioxane, the conformation equilibrium is shifted toward the trans-isomer with diaxial positions of the furyl and oxymethyl groups. The results of calculations suggest that the synthesis can lead to a cis-isomer with an axial orientation of the furyl and equatorial oxymethyl groups. It was shown experimentally that the synthesis leads to a mixture of trans- and cis-isomers. Mild conditions (room temperature, aqueous medium) lead to formation of the trans-isomer and small amounts of the cis-isomer (less than 2%). In rigid conditions (boiling in aromatic hydrocarbons), up to 20% of the cis-isomer is formed. 1998 Plenum Publishing Corporation.
